Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0221289
Disease: Synovioma, benign
Synovioma, benign
2 0 2 0.22 0 0
CUI: C0007815
Disease: Cerebrospinal Fluid Rhinorrhea
Cerebrospinal Fluid Rhinorrhea
3 0 2 0.20 0 0
CUI: C1847651
Disease: Rapidly progressive dementia
Rapidly progressive dementia
9 0 3 0.20 0 0
CUI: C0588125
Disease: Nodular tenosynovitis
Nodular tenosynovitis
10 0 3 0.19 0 0
Fibrous histiocytoma of tendon sheath
13 0 3 0.16 0 0
POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY 1
7 0 2 0.14 0 0
CUI: C0338455
Disease: Dementia of frontal lobe type
Dementia of frontal lobe type
20 0 3 0.12 0 0
CUI: C0235146
Disease: Euphoric mood
Euphoric mood
1 0 1 0.11 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe
1 0 1 0.11 0 0
CUI: C0270920
Disease: Supranuclear paralysis
Supranuclear paralysis
1 0 1 0.11 0 0
CUI: C0333419
Disease: Sarcoid type granuloma
Sarcoid type granuloma
1 0 1 0.11 0 0
CUI: C0333454
Disease: Granulovacuolar degeneration
Granulovacuolar degeneration
1 0 1 0.11 0 0
CUI: C0751421
Disease: Hemispatial Neglect
Hemispatial Neglect
1 0 1 0.11 0 0
CUI: C0751878
Disease: Vasculitis, Central Nervous System
Vasculitis, Central Nervous System
1 0 1 0.11 0 0
CUI: C0860515
Disease: Freezing of gait
Freezing of gait
1 0 1 0.11 0 0
CUI: C1836151
Disease: Frontolimbic dementia
Frontolimbic dementia
1 0 1 0.11 0 0
CUI: C1838313
Disease: Pick Complex
Pick Complex
1 0 1 0.11 0 0
Supranuclear Palsy, Progressive, 1, Atypical
1 0 1 0.11 0 0
PULMONARY ALVEOLAR PROTEINOSIS, ACQUIRED
1 0 1 0.11 0 0
CUI: C3888929
Disease: Cryptococcus gattii infection
Cryptococcus gattii infection
1 0 1 0.11 0 0
CUI: C4017292
Disease: GALACTOSIALIDOSIS, LATE INFANTILE
GALACTOSIALIDOSIS, LATE INFANTILE
1 0 1 0.11 0 0
CUI: C4017293
Disease: GALACTOSIALIDOSIS, ADULT
GALACTOSIALIDOSIS, ADULT
1 0 1 0.11 0 0
CUI: C4017294
Disease: GALACTOSIALIDOSIS, EARLY INFANTILE
GALACTOSIALIDOSIS, EARLY INFANTILE
1 0 1 0.11 0 0
CUI: C4021536
Disease: Mild conductive hearing impairment
Mild conductive hearing impairment
1 0 1 0.11 0 0
CUI: C4024962
Disease: Axial muscle stiffness
Axial muscle stiffness
1 0 1 0.11 0 0